Efficient diastereoselective synthesis of (2R,3R,4R)-2-amino-3-hydroxy-4,5- dimethylhexanoic acid, the lactone linkage unit of homophymine A

Chemical and Pharmaceutical Bulletin

Volumn 61, Issue 2, 2013, Pages 245-250

  Ohtaka, Junpei ^a   Hamajima, Akinari ^a   Nemoto, Tetsuhiro ^a   Hamada, Yasumasa ^a  

^a CHIBA UNIVERSITY   (Japan)

Author keywords

hydroxy amino acid; Anti selective asymmetric hydrogenation; Evans' asymmetric alkylation; Homophymine A

Indexed keywords

2 AMINO 3 HYDROXY 4,5 DIMETHYLHEXANOIC ACID; 2 HYDROXYIMINO 4,5 DIMETHYL 3 OXO HEXANOIC ACID; 2,3 DIMETHYL BUTYRIC ACID; 3 TERT BUTYL 4 METHYL 2,2 DIMETHYL 5 3 METHYLBUTAN 2 YL)OXAZOLIDINE 3,4 DICARBOXYLATE; 4 BENZYL 3 (3 METHYLBUTANOYL)OXAZOLIDIN 2 ONE; 4 BENZYL 3 2,3 DIMETHYLBUTANOYL)OXAZOLIDIN ONE; 4,5 DIMETHYL 3 OXO HEXANOIC ACID METHYL ESTER; ANTIVIRUS AGENT; METHYL 2 (TERT BUTOXYCARBONYLAMINO) 3 HYDROXY 4,5 DIMETHYLHEXANOATE; METHYL 2 AMINO 3 HYDROXY 4,5 DIMETHYLHEXANOATE HYDROCHLORIDE; METHYL 2 AMINO 4,5 DIMETHYL 3 OXOHEXANOATE HYDROCHLORIDE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGENATION; STEREOCHEMISTRY;

ALKYLATION; ANIMALS; DEPSIPEPTIDES; ESTERS; HYDROGENATION; LACTONES; PORIFERA; STEREOISOMERISM;

EID: 84873603577     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.c12-00944     Document Type: Article

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